85 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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WELL@HOME SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
20GA Straight Laser Probe, SMA905
FDA UDI
Peregrine Surgical, Llc·00632307001772·20GA Straight Laser Probe, SMA905
LEONE SPA
FDA UDI
LEONE SPA·08033707001973·LEOWIRE SPRING HARD 1,2mm
Ormco
FDA UDI
ORMCO CORPORATION·00889989024753·BONDABLE LINGUAL RETAINER CUSPID 2
n/a
FDA UDI
Ortho Development Corporation·00822409073771·10/12 Distal Reamer 12mm
Trulink
FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522126291·CO2 NASAL CANNULA, PEDIATRIC
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710820400120·Zadik Calcaneal Guide, 40mm x 12°
IMPRA CARBOFLO EPTFE VASCULAR GRAFTS
FDA 510(k)
FDA Class 2
·Cardiovascular
IMMULITE PHENOBARBITAL, MODELS LKPB1, LKPB5
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ENDOPATH
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC·Product code GEI·July 24, 2014
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·ACCULINK CAROTID STENT SYSTEM AND RX ACCULINK CAROTID STENT SYSTEM
PINNACLE MTL INS NEUT36IDX52OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·April 8, 2013
PFC SIGMA C/S NPOR FE LT SZ2.5
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIVISION OF DEPUY-ORTHOPAEDICS, INC.·Product code JWH·May 6, 2008
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·April 5, 2011
3I T3® WITH DCD® TAPERED IMPLANT 6/5 X 15MM
FDA Adverse Event
Injury
·BIOMET 3I·Product code DZE·July 10, 2019
3I T3® WITH DCD® TAPERED IMPLANT 6/5 X 15MM
FDA Adverse Event
Injury
·BIOMET 3I·Product code DZE·July 10, 2019
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·ACCULINK CAROTID STENT SYSTEM
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·RX ACCULINK AND ACCULINK CAROTID STENT SYSTEM
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·RX ACCULINK & ACCULINK CAROTID STENT SYSTEMS
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·RX ACCULINK & ACCULINK CAROTID STENT SYSTEMS